|
Symbol Name ID |
Sox9
SRY (sex determining region Y)-box 9 MGI:98371 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Conductive hearing impairment |
Low-set ears |
Hearing impairment |
| Disease(s) Associated with SOX9 | |||
| campomelic dysplasia |
| Mouse Phenotypes | hearing/vestibular/ear phenotype |
absent incus |
absent malleus |
absent stapes |
dilated cochlea |
dilated scala media |
small scala tympani |
abnormal endolymphatic duct morphology |
dilated endolymphatic duct |
abnormal otolith morphology |
decreased endocochlear potential |
nonsyndromic hearing impairment |
|
| Availability | Mouse Genotype | ||||||||||||
| Sox9Bbfc/Sox9+ | * | ||||||||||||
| Sox9tm1.2Ksec/Sox9+ | |||||||||||||
| Sox9tm2Crm/Sox9tm2Crm H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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| Sox9tm1.1Ksec/Sox9+ Tg(Rr141-cre)1Ksec/0 (conditional) |
* | ||||||||||||
| Sox9tm2Crm/Sox9+ Tg(Rr141-cre)1Ksec/0 (conditional) |
* | ||||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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